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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 901954Erstellt: 25. Oktober 2026

Sodium hydride → methyl 3-chloro(N-(4-chlorobenzenesulphonyl)-N-methylaminomethyl)thiophene-2-carboxylate

https://huagongshe.com/reaction/901954

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
Edukt4-Chloro-N-methylbenzenesulfonamideHCID 232992—
EduktPotassium bisulfateHCID 516920—
EduktMethyl 4-(bromomethyl)-3-chlorothiophene-2-carboxylateHCID 18376575—
LösungsmittelDimethylformamideHCID 6228—
Produktmethyl 3-chloro(N-(4-chlorobenzenesulphonyl)-N-methylaminomethyl)thiophene-2-carboxylateHCID 69208322102,3%

Reaktionsschritte

Sodium hydride (60% dispersion, 150 mg, 3.8 mmol) was added to a solution of 4-chloro-N-methylbenzenesulfonamide (640 mg, 3.1 mmol) in DMF (12 ml) while cooling in an ice/water bath. After stirring for 15 min the mixture was allowed to warm to room temperature and stirred for a further 30 min. Methyl 4-bromomethyl-3-chlorothiophene-2-carboxylate (1.08 g, 4.0 mmol) was added and the mixture was stirred for 18 h. 0.3N Potassium hydrogen sulphate solution was added and the mixture evaporated. The mixture was extracted with ethyl acetate and the organic extract was washed with brine, dried and reduced. Chromatography (25% EtOAc/75% 60-80 pet ether) yielded methyl 3-chloro(N-(4-chlorobenzenesulphonyl)-N-methylaminomethyl)thiophene-2-carboxylate (1.25 g, 79%) as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07365065B2
Quelldatensatzuspto-grants-2008_04
ORD IDord-337ed5aeaf244c55825edb2de5c57ca4
Quellennotizuspto-grants-2008_04